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8-Methyl-3-oxo-3,8-dihydro-1H-indeno<1,2-c>furan | 124583-42-2

中文名称
——
中文别名
——
英文名称
8-Methyl-3-oxo-3,8-dihydro-1H-indeno<1,2-c>furan
英文别名
3-oxo-8-methyl-1H,3H-indeno<1,2-c>furan;4-Methyl-3,4-dihydroindeno[1,2-c]furan-1-one
8-Methyl-3-oxo-3,8-dihydro-1H-indeno<1,2-c>furan化学式
CAS
124583-42-2
化学式
C12H10O2
mdl
——
分子量
186.21
InChiKey
QJPDYFGFYYPAKU-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    422.9±34.0 °C(Predicted)
  • 密度:
    1.26±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    8-Methyl-3-oxo-3,8-dihydro-1H-indeno<1,2-c>furan 生成 4-Methyl-3,3a,4,8b-tetrahydroindeno[1,2-c]furan-1-one
    参考文献:
    名称:
    Kasper Annette M., Nash John J., Morrison Harry, J. Org. Chem, 59 (1994) N 10, S 2792-2798
    摘要:
    DOI:
  • 作为产物:
    描述:
    2-Butynyl phenylacetate 在 rhodium(II) octanoate sodium hydride 、 甲烷磺酰基叠氮化物 作用下, 以 为溶剂, 反应 6.0h, 生成 8-Methyl-3-oxo-3,8-dihydro-1H-indeno<1,2-c>furan
    参考文献:
    名称:
    Rhodium(II)-catalyzed cyclization of 2-alkynyl 2-diazo-3-oxobutanoates as a method for synthesizing substituted furans
    摘要:
    A series of 2-alkynyl 2-diazo-3-oxobutanoates, when treated with a catalytic quantity of rhodium(II) acetate, were found to produce furo[3,4-c]furans in good yield. The reaction proceeds by addition of a rhodium-stabilized carbenoid onto the acetylenic pi-bond to give a vinyl carbenoid which subsequently cyclizes onto the neighboring carbonyl group to produce the furan ring. In a similar manner, indeno[1,2-c]furans were produced from 2-butynyl 2-diazoarylacetates. Compounds substituted with methyl groups on the propargylic carbon atom cyclized at a slower rate. This rate diminution is attributed to the fact that the unsubstituted propargyl group can more easily achieve the required conformation for cyclization. C-H insertion was found to compete with furan formation when an alkyl group was attached to the keto functionality of the starting diazo acetoacetate. Diazo alkynyl sulfones undergo a novel oxygen transfer reaction when treated with rhodium(II) acetate at 80-degrees-C. The cyclized product is formed by sulfone oxygen attack onto the vinyl carbenoid producing a dipolar species which subsequently collapses to give the butenolide sulfoxide.
    DOI:
    10.1021/jo00053a009
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文献信息

  • Preparation of oxygenated heterocycles via the cyclization reaction of α-diazo substituted alkynes
    作者:Frederick R. Kinder、Albert Padwa
    DOI:10.1016/s0040-4039(00)97184-3
    日期:1990.1
  • Spectroscopy and Photochemistry of Phenylacetic Acid Esters and Related Substrates. The Stereoelectronic Dependence of the Aryl/Carboxyl Bichromophore Interaction
    作者:Annette M. Kasper、John J. Nash、Harry Morrison
    DOI:10.1021/jo00089a025
    日期:1994.5
    The 254-nm-initiated Norrish Type II photofragmentation of the ethoxyethyl esters of a series of phenylacetic acids (1b-4b) has been studied in order to further elaborate the aryl/ester interaction that is photochemically and photophysically evident in these systems. The ethoxyethyl ester of benzonorbornene-1-carboxylic acid (5) has also been prepared and studied, as has a rigid tricyclic lactone (6) which places the chromophores in an optimal stereoelectronic relationship for interaction. The experimental work is accompanied by Hartree-Fock (HF), Natural Bond Orbital (NBO), and Configuration Interaction with Single Excitations (CIS) calculations on the methyl esters of phenylacetic acid (1a) and alpha-methoxyphenylacetic acid (4a). The calculations confirm extensive through-space (TS) and through-bond (TB) interactions between the aryl and ester pi* orbitals but fail to provide conformational or electronic arguments to explain the unusually high reactivity of the alpha-methoxy series.
  • Generation of vinylcarbenes by the intramolecular addition of .alpha.-diazo ketones to acetylenes
    作者:Albert Padwa、Ugo Chiacchio、Yves Garreau、Jamal M. Kassir、Keith E. Krumpe、Allen M. Schoffstall
    DOI:10.1021/jo00289a006
    日期:1990.1
  • PADWA, ALBERT;CHIACCHIO, UGO;GARREAU, YVES;KASSIR, JAMAL M.;KRUMPE, KEITH+, J. ORG. CHEM., 90,(1990) N, C. 414-416
    作者:PADWA, ALBERT、CHIACCHIO, UGO、GARREAU, YVES、KASSIR, JAMAL M.、KRUMPE, KEITH+
    DOI:——
    日期:——
  • KINDER, FREDERICK R.;PADWA, ALBERT, TETRAHEDRON LETT., 31,(1990) N7, C. 6835-6838
    作者:KINDER, FREDERICK R.、PADWA, ALBERT
    DOI:——
    日期:——
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